CO4950556A1 - QUINOLINE DERIVATIVES THAT HAVE A GROUP IMIDAZOLE AND COMPOSITIONS THAT CONTAIN THEM. - Google Patents
QUINOLINE DERIVATIVES THAT HAVE A GROUP IMIDAZOLE AND COMPOSITIONS THAT CONTAIN THEM.Info
- Publication number
- CO4950556A1 CO4950556A1 CO98037149A CO98037149A CO4950556A1 CO 4950556 A1 CO4950556 A1 CO 4950556A1 CO 98037149 A CO98037149 A CO 98037149A CO 98037149 A CO98037149 A CO 98037149A CO 4950556 A1 CO4950556 A1 CO 4950556A1
- Authority
- CO
- Colombia
- Prior art keywords
- group
- compositions
- contain
- ncn
- quinoline derivatives
- Prior art date
Links
Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D233/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings
- C07D233/04—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
- C07D401/06—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P19/00—Drugs for skeletal disorders
- A61P19/02—Drugs for skeletal disorders for joint disorders, e.g. arthritis, arthrosis
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P37/00—Drugs for immunological or allergic disorders
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P37/00—Drugs for immunological or allergic disorders
- A61P37/02—Immunomodulators
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/10—Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
- C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
- C07D403/06—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
- C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
- C07D403/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D409/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
- C07D409/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing three or more hetero rings
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- Animal Behavior & Ethology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Pharmacology & Pharmacy (AREA)
- Engineering & Computer Science (AREA)
- Immunology (AREA)
- Neurology (AREA)
- Heart & Thoracic Surgery (AREA)
- Cardiology (AREA)
- Vascular Medicine (AREA)
- Biomedical Technology (AREA)
- Urology & Nephrology (AREA)
- Neurosurgery (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Rheumatology (AREA)
- Physical Education & Sports Medicine (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
Abstract
Un compuesto de la fórmula I o IIcaracterizado porque:1, m, r, s y t son 0 ó 1;n es 0, 1 ó 2;y se selecciona del grupo que consiste de CHR12 , SO2 , SO3 , CO , CO2 , O, NR13 , SO2 NR14 , CONR15 , C(NCN), C(NCN)NR16 , NR17 CO, NR18 SO2 , CONR19 NR20 , SO2 NR21 NR22 , S(O)(NR23 ), S(NR24 ) (NR25 ), o sin Y;Z se selecciona del grupo que consiste de CR12 , S, SO, SO2 , SO3 , CO, CO2 , O, NR13 , SO2 NR14 , CONR15 , NR26 NR27 , ONR28 , NR29 O, NR30 SO2 NR31 , NR32 SO2 , NR33 C(NCN), NR34 C(NCN)NR35 , NR36 CO, NR37 CONR38 , NR39 CO2 , OCONR40 , S(O)(NR41 ), S(NR42 ) NR43 ) o CHR12 ; o sin Z;R7 , R8 se seleccionan del grupo que consiste de hidrógeno halo, nitro, ciano y U-R44 ;U se selecciona del grupo que consiste de S, O, NR45 , CO, SO, SO2 , CO2 , NR46 CO2 , NR47 CONR48 , NR49 SO2 , NR50 SO2 NR51 , SO2 NR52 , NR53 CO, CONR54 , PO2 R55 y PO3 R56 o sin U;R9 , R10 , R12 , R13 , R14 , R15 , R16 , R17 , R18 , R19 , R20 , R21 , R22 , R23 , R24 , R25 ,R26 , R27 , R28 , R29 , R30 , R31 , R32 , R33 , R34 , R35 , R36 , R37 , R38 , R39 , R40 , R41 , R42 , R43 , R44 , R45 , R46 , R47 , R48 , R49 , R50 , R51 , R52 , R53 , R54 , R55 , R56 , R57 , R58 , R59 , se seleccionan del grupo que consiste de hidrógeno, alquilo inferior, arilo, heterociclo, alquilo sustituido o arilo;R11 y R44 se seleccionan del grupo que consiste de hidrógeno, alquilo, alquilo sustituido, alquenilo, alquenilo sustituido, alquinilo, alquinilo sustituido, aralquilo, cicloalquilo, arilo,...A compound of formula I or II characterized in that: 1, m, r, s and t are 0 or 1; n is 0, 1 or 2; and is selected from the group consisting of CHR12, SO2, SO3, CO, CO2, O, NR13, SO2 NR14, CONR15, C (NCN), C (NCN) NR16, NR17 CO, NR18 SO2, CONR19 NR20, SO2 NR21 NR22, S (O) (NR23), S (NR24) (NR25), or without Y ; Z is selected from the group consisting of CR12, S, SO, SO2, SO3, CO, CO2, O, NR13, SO2 NR14, CONR15, NR26 NR27, ONR28, NR29 O, NR30 SO2 NR31, NR32 SO2, NR33 C ( NCN), NR34 C (NCN) NR35, NR36 CO, NR37 CONR38, NR39 CO2, OCONR40, S (O) (NR41), S (NR42) NR43) or CHR12; or without Z; R7, R8 are selected from the group consisting of halo, nitro, cyano and U-R44 hydrogen; U is selected from the group consisting of S, O, NR45, CO, SO, SO2, CO2, NR46 CO2, NR47 CONR48, NR49 SO2, NR50 SO2 NR51, SO2 NR52, NR53 CO, CONR54, PO2 R55 and PO3 R56 or without U; R9, R10, R12, R13, R14, R15, R16, R17, R18, R19, R20, R21 , R22, R23, R24, R25, R26, R27, R28, R29, R30, R31, R32, R33, R34, R35, R36, R37, R38, R39, R40, R41, R42, R43, R44, R45, R46 , R47, R48, R49, R50, R51, R52, R53, R54, R55, R56, R57, R58, R59, are selected from the group consisting of hydrogen, lower alkyl, aryl, heterocycle, substituted alkyl or aryl; R11 and R44 are selected from the group consisting of hydrogen, alkyl, substituted alkyl, alkenyl, substituted alkenyl, alkynyl, substituted alkynyl, aralkyl, cycloalkyl, aryl, ...
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US5159497P | 1997-07-02 | 1997-07-02 |
Publications (1)
Publication Number | Publication Date |
---|---|
CO4950556A1 true CO4950556A1 (en) | 2000-09-01 |
Family
ID=21972255
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CO98037149A CO4950556A1 (en) | 1997-07-02 | 1998-07-01 | QUINOLINE DERIVATIVES THAT HAVE A GROUP IMIDAZOLE AND COMPOSITIONS THAT CONTAIN THEM. |
Country Status (24)
Country | Link |
---|---|
US (2) | US6387926B1 (en) |
EP (1) | EP0994856A4 (en) |
JP (1) | JP2002507989A (en) |
KR (1) | KR100385941B1 (en) |
CN (1) | CN1261880A (en) |
AR (1) | AR016304A1 (en) |
AU (1) | AU734721B2 (en) |
BR (1) | BR9810465A (en) |
CA (1) | CA2294530A1 (en) |
CO (1) | CO4950556A1 (en) |
HU (1) | HUP0004148A3 (en) |
ID (1) | ID24076A (en) |
IL (1) | IL133470A0 (en) |
MY (1) | MY117961A (en) |
NO (1) | NO316117B1 (en) |
NZ (1) | NZ501293A (en) |
PE (1) | PE86599A1 (en) |
PL (1) | PL337697A1 (en) |
RU (1) | RU2211838C2 (en) |
TR (1) | TR199903331T2 (en) |
TW (1) | TW527355B (en) |
UY (1) | UY25074A1 (en) |
WO (1) | WO1999001434A1 (en) |
ZA (1) | ZA985778B (en) |
Families Citing this family (47)
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AU2478500A (en) | 1998-12-08 | 2000-06-26 | Merck & Co., Inc. | Inhibitors of prenyl-protein transferase |
AU2477400A (en) | 1998-12-08 | 2000-06-26 | Merck & Co., Inc. | Inhibitors of prenyl-protein transferase |
MXPA02006474A (en) * | 1999-12-28 | 2002-11-29 | Eisai Co Ltd | Heterocyclic compounds having sulfonamide groups. |
GB0023915D0 (en) * | 2000-09-29 | 2000-11-15 | Inst Of Ophthalmology | Treatment of neuroinflammatory disease |
DK1339407T3 (en) * | 2000-11-28 | 2006-08-14 | Janssen Pharmaceutica Nv | Farnesyl protein transferase inhibitors for the treatment of inflammatory bowel disease |
FR2819510B1 (en) * | 2001-01-18 | 2003-10-31 | Servier Lab | NOVEL CYCLO [C] AZEPANE COMPOUNDS, PROCESS FOR THEIR PREPARATION AND THE PHARMACEUTICAL COMPOSITIONS CONTAINING THE SAME |
FR2819512B1 (en) * | 2001-01-18 | 2003-02-21 | Servier Lab | NOVEL CYCLO [D] AZEPANE COMPOUNDS, PROCESS FOR THEIR PREPARATION AND PHARMACEUTICAL COMPOSITIONS CONTAINING THEM |
FR2825705B1 (en) * | 2001-06-08 | 2005-05-20 | Aventis Pharma Sa | NOVEL HETEROCYCLIC COMPOUNDS, THEIR PREPARATION AND THEIR USE AS MEDICAMENTS, IN PARTICULAR AS ANTI-BACTERIANS |
US6740757B2 (en) * | 2001-08-29 | 2004-05-25 | Pfizer Inc | Enantiomers of 6-[(4-chloro-phenyl)-hydroxy-(3-methyl-3h-imidazol-4-yl)-methyl]-4-[3-(3-hydroxy-3-methyl-but-1-ynyl)-phenyl]-1-methyl-1h-quinolin-2-one and salts thereof, useful in the treatment of cancer |
FR2835186B1 (en) | 2002-01-28 | 2006-10-20 | Aventis Pharma Sa | NOVEL HETEROCYCLIC COMPOUNDS ACTIVE AS BETA-LACTAMASES INHIBITORS |
AU2003259717A1 (en) * | 2002-08-07 | 2004-02-25 | Bristol-Myers Squibb Company | Modulators of rabggt and methods of use thereof |
FR2844273B1 (en) | 2002-09-05 | 2008-04-04 | Aventis Pharma Sa | NOVEL HETEROCYCLIC COMPOUNDS, METHOD AND INTERMEDIARY PREPARATION AND USE AS MEDICAMENT, IN PARTICULAR AS INHIBITORS OF BETA-LACTAMASES AND ANTI-BACTERIALS. |
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EP1644335A4 (en) | 2003-07-11 | 2008-06-04 | Bristol Myers Squibb Co | Tetrahydroquinoline derivatives as cannabinoid receptor modulators |
CA2546727C (en) | 2003-11-20 | 2012-10-02 | Children's Hospital Medical Center | Gtpase inhibitors and methods of use |
US20070293539A1 (en) * | 2004-03-18 | 2007-12-20 | Lansbury Peter T | Methods for the treatment of synucleinopathies |
US20060106060A1 (en) * | 2004-03-18 | 2006-05-18 | The Brigham And Women's Hospital, Inc. | Methods for the treatment of synucleinopathies (Lansbury) |
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US20050288298A1 (en) * | 2004-03-18 | 2005-12-29 | The Brigham And Women's Hospital, Inc. | Methods for the treatment of synucleinopathies |
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US20060194821A1 (en) * | 2005-02-18 | 2006-08-31 | The Brigham And Women's Hospital, Inc. | Compounds inhibiting the aggregation of superoxide dismutase-1 |
US7662824B2 (en) | 2005-03-18 | 2010-02-16 | Janssen Pharmaceutica Nv | Acylhydrazones as kinase modulators |
KR101589551B1 (en) | 2005-07-15 | 2016-02-02 | 알바니 몰레큘라 리써치, 인크. | Aryl-and heteroaryl-substituted tetrahydrobenzazepines and use thereof to block reuptake of norepinephrine, dopamine, and serotonin |
CA2617056A1 (en) | 2005-07-29 | 2007-02-08 | Children's Hospital Medical Center | Gtpase inhibitors and methods of use and crystal structure of rac-1 gtpase |
US8003624B2 (en) * | 2005-08-25 | 2011-08-23 | Schering Corporation | Functionally selective ALPHA2C adrenoreceptor agonists |
CA2634598A1 (en) * | 2005-12-23 | 2007-07-05 | Link Medicine Corporation | Treatment of synucleinopathies |
ES2531190T3 (en) * | 2006-03-06 | 2015-03-11 | Japan Tobacco Inc | Method to produce a 4-oxoquinoline compound |
US20100137239A1 (en) * | 2006-04-24 | 2010-06-03 | Gloucester Pharmaceuticals | Gemcitabine combination therapy |
JP2010510184A (en) * | 2006-11-16 | 2010-04-02 | エフ.ホフマン−ラ ロシュ アーゲー | Substituted 4-imidazoles |
NZ580802A (en) * | 2007-05-10 | 2012-09-28 | Albany Molecular Res Inc | Aryloxy-and heteroaryloxy-substituted tetrahydrobenzazepines and use thereof to block reuptake of norepinephrine, dopamine, and serotonin |
FR2920773B1 (en) * | 2007-09-11 | 2009-10-23 | Servier Lab | 1,2,4,5-TETRAHYDRO-3H-BENZAZEPINES DERIVATIVES, PROCESS FOR THEIR PREPARATION AND PHARMACEUTICAL COMPOSITIONS CONTAINING THEM |
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US8232402B2 (en) * | 2008-03-12 | 2012-07-31 | Link Medicine Corporation | Quinolinone farnesyl transferase inhibitors for the treatment of synucleinopathies and other indications |
US20110060005A1 (en) * | 2008-11-13 | 2011-03-10 | Link Medicine Corporation | Treatment of mitochondrial disorders using a farnesyl transferase inhibitor |
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WO2013064231A1 (en) | 2011-10-31 | 2013-05-10 | Phenex Pharmaceuticals Ag | SEVEN-MEMBERED SULFONAMIDES AS MODULATORS OF RAR-RELATED ORPHAN RECEPTOR-GAMMA (RORγ, NR1F3) |
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1998
- 1998-05-26 TW TW087108171A patent/TW527355B/en not_active IP Right Cessation
- 1998-05-29 US US09/087,179 patent/US6387926B1/en not_active Expired - Lifetime
- 1998-06-16 KR KR10-1999-7012368A patent/KR100385941B1/en not_active IP Right Cessation
- 1998-06-16 RU RU2000102355/04A patent/RU2211838C2/en not_active IP Right Cessation
- 1998-06-16 BR BR9810465-9A patent/BR9810465A/en not_active IP Right Cessation
- 1998-06-16 TR TR1999/03331T patent/TR199903331T2/en unknown
- 1998-06-16 HU HU0004148A patent/HUP0004148A3/en unknown
- 1998-06-16 EP EP98930299A patent/EP0994856A4/en not_active Withdrawn
- 1998-06-16 CA CA002294530A patent/CA2294530A1/en not_active Abandoned
- 1998-06-16 AU AU79719/98A patent/AU734721B2/en not_active Ceased
- 1998-06-16 PL PL98337697A patent/PL337697A1/en unknown
- 1998-06-16 WO PCT/US1998/012549 patent/WO1999001434A1/en not_active Application Discontinuation
- 1998-06-16 JP JP50718899A patent/JP2002507989A/en not_active Ceased
- 1998-06-16 IL IL13347098A patent/IL133470A0/en unknown
- 1998-06-16 NZ NZ501293A patent/NZ501293A/en unknown
- 1998-06-16 CN CN98806818A patent/CN1261880A/en active Pending
- 1998-06-26 MY MYPI98002919A patent/MY117961A/en unknown
- 1998-06-26 PE PE1998000565A patent/PE86599A1/en not_active Application Discontinuation
- 1998-06-30 UY UY25074A patent/UY25074A1/en not_active IP Right Cessation
- 1998-07-01 ZA ZA9805778A patent/ZA985778B/en unknown
- 1998-07-01 CO CO98037149A patent/CO4950556A1/en unknown
- 1998-07-02 AR ARP980103223A patent/AR016304A1/en unknown
-
1999
- 1999-06-16 ID IDW991728A patent/ID24076A/en unknown
- 1999-12-30 NO NO19996571A patent/NO316117B1/en unknown
-
2000
- 2000-05-05 US US09/566,396 patent/US6602883B1/en not_active Expired - Fee Related
Also Published As
Publication number | Publication date |
---|---|
PL337697A1 (en) | 2000-08-28 |
US6387926B1 (en) | 2002-05-14 |
HUP0004148A3 (en) | 2002-09-30 |
NZ501293A (en) | 2001-10-26 |
UY25074A1 (en) | 2000-12-29 |
KR100385941B1 (en) | 2003-06-09 |
BR9810465A (en) | 2002-04-16 |
TR199903331T2 (en) | 2000-06-21 |
EP0994856A1 (en) | 2000-04-26 |
JP2002507989A (en) | 2002-03-12 |
NO996571L (en) | 2000-02-23 |
CA2294530A1 (en) | 1999-01-14 |
AU7971998A (en) | 1999-01-25 |
HUP0004148A2 (en) | 2001-10-28 |
PE86599A1 (en) | 1999-11-28 |
NO316117B1 (en) | 2003-12-15 |
US6602883B1 (en) | 2003-08-05 |
KR20010014258A (en) | 2001-02-26 |
ZA985778B (en) | 2000-01-20 |
TW527355B (en) | 2003-04-11 |
ID24076A (en) | 2000-07-06 |
NO996571D0 (en) | 1999-12-30 |
WO1999001434A1 (en) | 1999-01-14 |
EP0994856A4 (en) | 2000-12-06 |
CN1261880A (en) | 2000-08-02 |
IL133470A0 (en) | 2001-04-30 |
RU2211838C2 (en) | 2003-09-10 |
AU734721B2 (en) | 2001-06-21 |
AR016304A1 (en) | 2001-07-04 |
MY117961A (en) | 2004-08-30 |
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